Mobilization analysis of the dolmen of Dombate (Northwest Spain)

This paper presents an analysis of the mobilization of the dolmen of Dombate, a megalithic monument situated in the Northwest of Spain. The study is founded on simple static principles, with the application of basic concepts of soil mechanics (soil reactions were computed by the reaction modulus method) and rock mechanics (a simple secant approach was adopted to model the contact between orthostats). In addition, a simplified geometric model for dolmens was adopted. On the basis of these concepts, a numerical solver able to provide quick estimations of the system's mobilization was developed. Using this tool, a number of sensitivity analyses were conducted to estimate the mobilization that could be caused by a conservation project currently under consideration. It was found that mobilization might be excessive, and therefore, a safer procedure is proposed. In short, this paper puts forth a new rational approach for archaeological practices which may help to estimate the possible consequences of excavations and rehabilitations on megalithic structures.     

滇西北雪鸡坪斑岩铜矿流体包裹体初步研究

雪鸡坪中型斑岩铜矿床位于三江地区义敦岛弧南端的中甸弧,成矿斑岩为石英闪长玢岩和石英二长斑岩,属于印支期产物。含矿岩体蚀变分带明显,由中心向外发育强硅化带→石英绢云母化带→粘土化-石英绢云母化带→青磐岩化带,工业矿体赋存于斑岩体中心强硅化和石英绢云母化带内。矿化类型以网脉状矿化为主,细脉浸染状矿化不发育。本文对主要矿化阶段石英脉中的流体包裹体系统进行了包裹体岩相学、显微测温学和激光拉曼谱学研究,发现与成矿有关的流体包裹体可以分为水溶液包裹体、CO2包裹体和含子矿物包裹体3类,子矿物主要为石盐、方解石、赤铁矿和少量CaCl2水合物及不透明硫化物。其中含子矿物包裹体均一温度为230～420℃,盐度为33．48％～75．40％NaCl equiv．,密度为1．01～1．09g／cm^3。激光拉曼光谱分析表明,包裹体的液相成分主要为H2O,气相成分为H2O和CO2。早期水溶液包裹体和CO2包裹体共生,其均一温度相近,以及纯CO2包裹体的发现,指示成矿流体存在不混溶现象,这种不混溶是由原始岩浆流体“二次沸腾”作用产生的。CO2相分离、温压条件降低和pH值升高是雪鸡坪斑岩铜矿硫化物沉淀的主要原因。晚期低温、低盐度的流体可能来源于大气降水与岩浆流体的混和,对矿化的意义不大。     

洛川黄土-红粘土序列铁氧化物组成及其古气候指示

对洛川黄土、古土壤和红粘土中磁性矿物组成、成因和相关系进行了研究。结果表明:黄土磁性矿物以风尘磁铁矿为主,少量的成土赤铁矿和成土磁赤铁矿;古土壤磁性矿物以成土磁赤铁矿为主,成土赤铁矿次之,少量的风尘磁铁矿和赤铁矿;红粘土磁性矿物以成土赤铁矿为主,风尘磁铁矿和成土磁赤铁矿次之,少量风尘赤铁矿。黄土、古土壤和红粘土磁性矿物组成差异,反映了其形成期不同的古气候特性以及不同气候条件下生物地球化学作用强度的差异。干冷的冰期,黄土弱成土作用形成了以粗颗粒的风尘磁铁矿核 赤铁矿边的磁化率载体。间冰期的温暖湿润的古气候最有利于生物活动,强烈生物活动导致古土壤中大量纳米超细磁赤铁矿/磁铁矿产生,形成以磁赤铁矿为主,风尘磁铁矿核 赤铁矿边为辅的磁化率载体。红粘土成壤期,强降雨强蒸发的长干短湿的高温炎热的古气候使得红粘土化学风化强烈,生物地球化学活动较弱,形成以磁铁矿核 赤铁矿边和磁赤铁矿核 赤铁矿边的磁化率载体。黄土、古土壤和红粘土磁性矿物组成、磁性矿物相关系是其形成期独特的古气候指示。     

云贵高原湖泊沉积物─水界面碱度扩散通量研究

于1991-1995年间5次在云贵高原泸沽湖、洱海湖和贵州阿哈湖、百花湖的湖心采集沉积物柱芯、界面水和湖水样品，通过其pH值和HCO-3浓度剖面及界面碱度扩散通量的研究，首次定量评估高原湖泊界面扩散作用上覆水体碱度的影响程度。研究结果表明，云贵高原某些湖水寄宿时间相对较长、湖水深度相对小的湖泊，界面扩散作用是水体碱度的重要来源之一;湖水寄宿时间较短、深度较小的湖泊，界面扩散对上覆水体的影响可以忽略不计。     

海水中磷酸盐在固体粒子上阴离子交换作用 海水中磷酸盐-固体粒子相互作用的台阶型等温线

通过研究氯化钠溶液中磷酸盐在4种固体粒子（针铁矿、δ－氧化锰、伊利石和高岭石）上的交换等温线及钙对上述交换等温线的影响，发现磷酸盐液－固界面作用的台阶型等温线（2个台阶），可用分级离子／配位子交换等温式定量描述。钙能够促进磷酸盐在针铁矿和δ－氧化锰上的交换作用，其机理是交换在固体粒子上的钙再结合溶液中的磷酸盐，形成表面无机三元络合物。     

云贵高原湖泊沉积物─水界面碱度扩散通量研究

于１９９１－１９９５年间５次在云贵高原泸沽湖，洱海湖和贵州阿哈湖，百花湖的湖心采集沉积物柱芯，界面水和湖水样品，通过其ｐＨ值和ＨＣＯ３浓度剖面及界面碱度扩散通量的研究，首次定量评估高原湖泊界面扩散作用上不体碱度的影响程度，研究结果表明，云贵高原某些湖水寄宿时间对较长，湖水深度相对小的湖泊，界面扩散作用是水体碱度的重要来源之一，湖水寄宿时间较短，深度较小的湖泊，界面扩散对上覆水体的影响可以忽略不地。     

青藏高原东部多年冻土退化对环境的影响

退化是本区多年冻土变化的基本趋势，不同区段退化幅度有差异，影响退化的因素除了全球气候转暖外，还有局地气候和地下水迳流。在退化敏感的地带，工程建设，牧区生态平衡都有不可忽视的影响。     

引入差比关系法分析西北太平洋TOPEX/POSEIDON卫星高度计测高数据

TOPEX/POSEIDON(T/P)卫星高度计数据信息中存在周期成分混淆问题.对其中的一类混淆引入差比关系方法对混淆的分潮进行分离.卫星轨道交叉点资料包括升轨和降轨资料,资料量比沿轨点资料多1倍,经分析发现:在已有为期6a多的观测资料时间序列中,在沿轨处混淆的分潮如K₁和SSA在交叉点处不再混淆,可以直接分离.因此首先对交叉点资料进行调和分析.然后由交叉点的分析结果得到分潮间的差比关系,处理到相近的沿轨点处,从而得到沿轨点的调和常数.用引入差比关系方法,对西北太平洋海区6a多的T/P卫星高度计资料进行了潮汐分析,并与沿岸及岛屿验潮站资料进行了比较,所得结果较满意.     

Determination of phospholipid fatty acid structures and stable carbon isotope compositions of deep-sea sediments of the Northwest Pacific, ODP site 1179

Sediment samples ranging from 0.05 to 278 m below sea floor (mbsf) at a Northwest Pacific deep-water (5564 mbsl) site (ODP Leg 191, Site 1179) were analyzed for phospholipid fatty acids (PLFAs). Total PLFA concentrations decreased by a factor of three over the first meter of sediment and then decreased at a slower rate to approximately 30 mbsf. The sharp decrease over the first meter corresponds to the depth of nitrate and Mn(IV) reduction as indicated by pore water chemistry. PLFA-based cell numbers at site 1179 had a similar depth profile as that for Acridine orange direct cell counts previously made on ODP site 1149 sediments which have a similar water depth and lithology. The mole percentage of straight chain saturated PLFAs increases with depth, with a large shift between the 0.95 and 3.95 mbsf samples. PLFA stable carbon isotope ratios were determined for sediments from 0.05 to 4.53 mbsf and showed a general trend toward more depleted δ¹³C values with depth. Both of these observations may indicate a shift in the bacterial community with depth across the different redox zones inferred from pore water chemistry data. The PLFA 10me16:0, which has been attributed to the bacterial genera Desulfobacter in many marine sediments, showed the greatest isotopic depletion, decreasing from − 20 to − 35‰ over the first meter of sediment. Pore water chemistry suggested that sulfate reduction was absent or minimal over this same sediment interval. However, 10me16:0 has been shown to be produced by recently discovered anaerobic ammonium oxidizing (anammox) bacteria which are known chemoautotrophs. The increasing depletion in δ¹³C of 10me16:0 with the unusually lower concentration of ammonium and linear decrease of nitrate concentration is consistent with a scenario of anammox bacteria mediating the oxidation of ammonium via nitrite, an intermediate of nitrate reduction.